Hs02164428_cn

• Gene Symbol: KRT32
• Assay Reference Genome Location: Chr.17:41464303 on build GRCh38
• Cytoband: 17q21.2

Target Gene Details

• Entrez Gene ID: 3882
• Gene Name: keratin 32
• Gene Aliases: HA2, HKA2, KRTHA2, hHa2
• Location: Chr.17:41459513-41469252 on Build GRCh38
• Assay Gene Location: Overlaps Intron 4 - Exon 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
KRT32	NM_002278.3			NP_002269.3
	X81419.1			CAA57179.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv510711	Chr.17:41455775 - 41574964 on Build GRCh38	Deletion	KRT35 KRT13 LINC00974 KRT32 KRT36 KRT19 MIR6510 KRT15 KRT9
nsv483014	Chr.17:41339595 - 41514244 on Build GRCh38	Loss	KRT31 KRT33B KRT38 KRT35 KRT13 KRT32 KRT36 KRT34 KRT37 KRT33A LOC100505782 KRT15
esv2758690	Chr.17:41145123 - 41740591 on Build GRCh38	Gain+Loss	KRTAP9-6 KRTAP17-1 KRT14 EIF1 KRT13 KRTAP4-3 KRT32 KRT34 KRT19 KRTAP9-3 LOC100505782 LINC00974 KRTAP9-1 KRTAP9-4 KRT15 KRT31 KRTAP9-7 KRT33B KRTAP9-8 KRT42P HAP1 KRT35 KRTAP16-1 KRTAP4-2 KRT17 KRTAP4-4 KRT9 KRTAP9-2 KRTAP4-1 KRT38 KRTAP4-5 KRTAP9-9 KRT16 KRT36 KRT37 MIR6510 KRTAP29-1 KRT33A GAST

More Information

Additional Information:

For this assay, SNP(s) [rs72830046] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

epidermis development

Function(s)

structural molecule activity